KR20200090815A - 안정화된, 충전된 폴리카르보네이트 조성물 - Google Patents
안정화된, 충전된 폴리카르보네이트 조성물 Download PDFInfo
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- KR20200090815A KR20200090815A KR1020207017109A KR20207017109A KR20200090815A KR 20200090815 A KR20200090815 A KR 20200090815A KR 1020207017109 A KR1020207017109 A KR 1020207017109A KR 20207017109 A KR20207017109 A KR 20207017109A KR 20200090815 A KR20200090815 A KR 20200090815A
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- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 239000002478 γ-tocopherol Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L69/00—Compositions of polycarbonates; Compositions of derivatives of polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/04—Anhydrides, e.g. cyclic anhydrides
- C08F222/06—Maleic anhydride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F222/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a carboxyl radical and containing at least one other carboxyl radical in the molecule; Salts, anhydrides, esters, amides, imides, or nitriles thereof
- C08F222/36—Amides or imides
- C08F222/40—Imides, e.g. cyclic imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/04—Homopolymers or copolymers of esters
- C08L33/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, which oxygen atoms are present only as part of the carboxyl radical
- C08L33/10—Homopolymers or copolymers of methacrylic acid esters
- C08L33/12—Homopolymers or copolymers of methyl methacrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L33/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- C08L33/24—Homopolymers or copolymers of amides or imides
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K5/00—Casings, cabinets or drawers for electric apparatus
- H05K5/02—Details
- H05K5/03—Covers
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K7/00—Constructional details common to different types of electric apparatus
- H05K7/20—Modifications to facilitate cooling, ventilating, or heating
- H05K7/2039—Modifications to facilitate cooling, ventilating, or heating characterised by the heat transfer by conduction from the heat generating element to a dissipating body
- H05K7/20436—Inner thermal coupling elements in heat dissipating housings, e.g. protrusions or depressions integrally formed in the housing
- H05K7/20445—Inner thermal coupling elements in heat dissipating housings, e.g. protrusions or depressions integrally formed in the housing the coupling element being an additional piece, e.g. thermal standoff
- H05K7/20472—Sheet interfaces
- H05K7/20481—Sheet interfaces characterised by the material composition exhibiting specific thermal properties
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2227—Oxides; Hydroxides of metals of aluminium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2237—Oxides; Hydroxides of metals of titanium
- C08K2003/2241—Titanium dioxide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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EP17208724.9 | 2017-12-20 | ||
EP17208724.9A EP3502182B1 (fr) | 2017-12-20 | 2017-12-20 | Compositions de polycarbonate chargées et stabilisées |
PCT/EP2018/084543 WO2019121229A1 (fr) | 2017-12-20 | 2018-12-12 | Compositions de polycarbonate chargées et stabilisées |
Publications (1)
Publication Number | Publication Date |
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KR20200090815A true KR20200090815A (ko) | 2020-07-29 |
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ID=60953536
Family Applications (1)
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KR1020207017109A KR20200090815A (ko) | 2017-12-20 | 2018-12-12 | 안정화된, 충전된 폴리카르보네이트 조성물 |
Country Status (7)
Country | Link |
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US (1) | US11345812B2 (fr) |
EP (1) | EP3502182B1 (fr) |
JP (1) | JP7225240B2 (fr) |
KR (1) | KR20200090815A (fr) |
CN (1) | CN111465654B (fr) |
TW (1) | TW201936779A (fr) |
WO (1) | WO2019121229A1 (fr) |
Families Citing this family (2)
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CN113614171B (zh) | 2019-03-28 | 2023-11-10 | 科思创知识产权两合公司 | 具有小的热膨胀的填充聚碳酸酯组合物 |
CN117529526A (zh) * | 2021-06-18 | 2024-02-06 | 科思创德国股份有限公司 | 具有高cti的阻燃聚碳酸酯组合物 |
Family Cites Families (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1007996B (de) | 1955-03-26 | 1957-05-09 | Bayer Ag | Verfahren zur Herstellung thermoplastischer Kunststoffe |
US2991273A (en) | 1956-07-07 | 1961-07-04 | Bayer Ag | Process for manufacture of vacuum moulded parts of high molecular weight thermoplastic polycarbonates |
US3148172A (en) | 1956-07-19 | 1964-09-08 | Gen Electric | Polycarbonates of dihydroxyaryl ethers |
US2999846A (en) | 1956-11-30 | 1961-09-12 | Schnell Hermann | High molecular weight thermoplastic aromatic sulfoxy polycarbonates |
DE1077872B (de) | 1958-03-22 | 1960-03-17 | Roehm & Haas Gmbh | Verfahren zur Herstellung Stickstoff enthaltender Derivate der Polymethacrylsaeure |
US2999835A (en) | 1959-01-02 | 1961-09-12 | Gen Electric | Resinous mixture comprising organo-polysiloxane and polymer of a carbonate of a dihydric phenol, and products containing same |
GB1122003A (en) | 1964-10-07 | 1968-07-31 | Gen Electric | Improvements in aromatic polycarbonates |
US3360498A (en) * | 1965-06-23 | 1967-12-26 | Mobay Chemical Corp | Stabilized polycarbonates |
NL152889B (nl) | 1967-03-10 | 1977-04-15 | Gen Electric | Werkwijze ter bereiding van een lineair polycarbonaatcopolymeer, alsmede orienteerbare textielvezel van dit copolymeer. |
DE2036052A1 (en) | 1970-07-21 | 1972-01-27 | Milchwirtschafthche Forschungs und Untersuchungs Gesellschaft mbH, 2100 Hamburg | Working up of additives in fat and protein - contng foodstuffs |
DE2063050C3 (de) | 1970-12-22 | 1983-12-15 | Bayer Ag, 5090 Leverkusen | Verseifungsbeständige Polycarbonate, Verfahren zu deren Herstellung und deren Verwendung |
DE2211956A1 (de) | 1972-03-11 | 1973-10-25 | Bayer Ag | Verfahren zur herstellung verseifungsstabiler blockcopolycarbonate |
US4049614A (en) * | 1975-10-20 | 1977-09-20 | Mobay Chemical Corporation | Pigmented polycarbonates |
CA1084193A (fr) * | 1975-10-20 | 1980-08-19 | Arthur L. Baron | Polycarbonates pigmentes contenant de la silice de taille micronique comme stabilisant |
JPS6232140A (ja) * | 1985-08-05 | 1987-02-12 | Mitsubishi Rayon Co Ltd | 熱可塑性樹脂組成物 |
JPS63221155A (ja) * | 1987-03-10 | 1988-09-14 | Toray Ind Inc | 熱可塑性樹脂組成物 |
CA1326922C (fr) * | 1988-03-10 | 1994-02-08 | Akihiro Wada | Composition de resine |
ATE159960T1 (de) | 1988-07-11 | 1997-11-15 | Gen Electric | Verfahren zur herstellung von polycarbonaten |
DE3832396A1 (de) | 1988-08-12 | 1990-02-15 | Bayer Ag | Dihydroxydiphenylcycloalkane, ihre herstellung und ihre verwendung zur herstellung von hochmolekularen polycarbonaten |
NO170326C (no) | 1988-08-12 | 1992-10-07 | Bayer Ag | Dihydroksydifenylcykloalkaner |
TW222292B (fr) | 1991-02-21 | 1994-04-11 | Ciba Geigy Ag | |
DE4238123C2 (de) | 1992-11-12 | 2000-03-09 | Bayer Ag | Verfahren zur Herstellung von thermoplastischen Polycarbonaten |
CN1046707C (zh) | 1994-11-10 | 1999-11-24 | 巴斯福股份公司 | 2-氰基丙烯酸酯 |
US5717057A (en) | 1994-12-28 | 1998-02-10 | General Electric Company | Method of manufacturing polycarbonate |
EP0839623B1 (fr) | 1996-10-30 | 2001-01-31 | Ciba SC Holding AG | Combinaison de stabilisateurs pour le procédé rotomolding |
DE19933132A1 (de) | 1999-07-19 | 2001-01-25 | Bayer Ag | Verfahren zur Herstellung von modifizierten Polycarbonaten |
DE10006208A1 (de) | 2000-02-11 | 2001-08-16 | Bayer Ag | IR-absorbierende Zusammensetzungen |
DE10022037A1 (de) | 2000-05-05 | 2001-11-08 | Bayer Ag | IR-absorbierende Zusammensetzungen |
DE10300598A1 (de) | 2003-01-10 | 2004-07-22 | Bayer Ag | Verfahren zur Herstellung von Polycarbonaten |
DE10311437A1 (de) * | 2003-03-15 | 2004-09-23 | Degussa Ag | Laser-Sinter-Pulver mit PMMI, PMMA und/oder PMMI-PMMA-Copolymeren, Verfahren zu dessen Herstellung und Formkörper, hergestellt aus diesem Laser-Sinterpulver |
US20050165148A1 (en) | 2004-01-28 | 2005-07-28 | Bogerd Jos V.D. | Infra-red radiation absorption articles and method of manufacture thereof |
CN101151321B (zh) | 2005-03-28 | 2012-05-23 | 三菱工程塑料株式会社 | 聚碳酸酯树脂组合物和热辐射遮蔽性成形体 |
US20060287422A1 (en) | 2005-06-16 | 2006-12-21 | General Electric Company | Thermoplastic polycarbonate compositions with improved mechanical properties, articles made therefrom and method of manufacture |
DE102005058847A1 (de) | 2005-12-09 | 2007-06-14 | Bayer Materialscience Ag | Polycarbonat-Formmassen |
JP5250349B2 (ja) | 2008-09-11 | 2013-07-31 | 日立オートモティブシステムズ株式会社 | 制動力制御装置 |
DE102009015040A1 (de) * | 2009-03-26 | 2010-09-30 | Bayer Materialscience Ag | (Co)polycarbonate mit verbesserten optischen Eigenschaften |
DE102009043510A1 (de) | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | Polycarbonatzusammensetzungen mit verbesserter Schmelzstabilität |
DE102009043513A1 (de) | 2009-09-30 | 2011-03-31 | Bayer Materialscience Ag | Polycarbonatzusammensetzungen mit verbesserten optischen Eigenschaften |
ITRM20100225A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione di polimeri con caratteristiche di assorbimento del calore e migliorate caratteristiche di colore. |
ITRM20100228A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione polimerica con caratteristiche di assorbimento del calore e migliorate caratteristiche di colore. |
ITRM20100227A1 (it) | 2010-05-10 | 2011-11-10 | Bayer Materialscience Ag | Composizione polimerica con caratteristiche di assorbimento di calore ad alta stabilità. |
CA2853186A1 (fr) | 2011-10-26 | 2013-05-02 | Bayer Intellectual Property Gmbh | Compositions de polycarbonate stabilisees comprenant des melanges d'acide silicique et d'un acide inorganique |
EP3043703A1 (fr) | 2013-09-11 | 2016-07-20 | Koninklijke Philips N.V. | Appareil d'imagerie mpi avec mouvement rapide du champ de vision |
JP6621739B2 (ja) | 2013-10-08 | 2019-12-18 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトCovestro Deutschland Ag | 弱酸の塩を用いてポリシロキサン−ポリカーボネートブロック共縮合物を調製する方法 |
WO2016087477A1 (fr) | 2014-12-04 | 2016-06-09 | Covestro Deutschland Ag | Compositions de polycarbonate contenant des cires de polyéthylène |
CN107163447A (zh) * | 2017-07-12 | 2017-09-15 | 合肥思博特软件开发有限公司 | 一种电子设备的外壳材料及其制备方法 |
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2017
- 2017-12-20 EP EP17208724.9A patent/EP3502182B1/fr active Active
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- 2018-12-12 WO PCT/EP2018/084543 patent/WO2019121229A1/fr active Application Filing
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- 2018-12-12 JP JP2020534264A patent/JP7225240B2/ja active Active
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- 2018-12-12 US US16/956,699 patent/US11345812B2/en active Active
- 2018-12-18 TW TW107145615A patent/TW201936779A/zh unknown
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US11345812B2 (en) | 2022-05-31 |
CN111465654A (zh) | 2020-07-28 |
EP3502182A1 (fr) | 2019-06-26 |
EP3502182B1 (fr) | 2020-10-21 |
CN111465654B (zh) | 2023-01-03 |
WO2019121229A1 (fr) | 2019-06-27 |
US20200332114A1 (en) | 2020-10-22 |
TW201936779A (zh) | 2019-09-16 |
JP2021507060A (ja) | 2021-02-22 |
JP7225240B2 (ja) | 2023-02-20 |
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